Description
Introduction
The product is suitable for sleep breathing,SpO2 monitoring.Suitable for family,community medical institutions and hospitals.
Features
1) SpO2 and PR value display, pulse sound and bar graph indication.
2) Pulse waveform and nose flow waveform display
3) Alarms for low power, finger out and exceeding limits
4) Battery status indication
5) Real-time clock
6) Timing power on/off
7) Storage of multiple cases
8) Continuous 12 hours data record
9) Uploading data via USB port
10) PC analysis software
Performance
◆ Nose air flow measurement range: 0 rpm~40 rpm, accuracy: ±2 rpm.
◆ SpO2 measurement range: 0%~100% (resolution 1%), accuracy: 70%~100%, ±2; less than 70%, unspecified.
◆ PR measurement range: 30 bpm~250 bpm, accuracy: ±2 or ±2% (whichever is greater).
◆ Resistance to surrounding light: The deviation between the value measured in the condition of man-made light or indoor natural light and that of darkroom is less than ±1%.
◆ Accuracy under low perfusion: low perfusion 0.4 %, SpO2 accuracy: ± 4 %; PR accuracy: ± 2 bpm or ± 2 %, whichever is greater.
◆ Power consumption: ≤100 mA.
◆ Power supply: 3.7 V rechargeable lithium battery.
◆ Safety type: internally powered equipment, type BF applied part.
Accessories
◆ A power adapter（optional）
◆ A USB data line
◆ A Nasal cannula
◆ Two Luer male taper
◆ Two kinds of SpO2 probes
◆ A User Manual
Physical characteristic
Dimension: 69 mm (L)×50mm (W) ×17.3 mm (H)
Weight: about 100g
Payment
We accept Paypal Payment.
Shipping
- Clearance: we will ship your item to your Ebay confirmed address.
- Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
Terms of Sale
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The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.If the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item. If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health.
The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE,TUV of Europe.The Fingertip Pulse Oximeter that is FDA 510K Approved.
About Us
Contec Medical Systems Co.,Ltd; 20 Years manufacturer,we have stock in USA and China.
Contact Us
Please contact us through eBay Message, we are on line to reply your message within 24 hours.
Whatsapp/Wechat:+86 18716007715;tessy.zhang@contecmed.com